Allele Registry

Canonical Allele Identifier: PA2826658401

Gene: LMNA HGNC NCBI

ClinVar Allele:

29518

ClinVar RCV:

RCV000015566

RCV000015567

RCV000057359

ClinVar Variation:

14479

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269554.1:p.Arg60Gly	CA017722 NM_001282625.2:c.178C>G